Integration across different omics datasets
Andrej Blejec
28. 4. 2024
1 Introduction
[Needs more text]
In this document we present a work-flow for integration across different omics datasets.
[Note] This is not the final version of the document.
2 Packages and files
A package with regularized CCA and multiomics DIABLO method is mixOmics. Package igraph is needed for network analysis.
library(mixOmics)
library(igraph)Package for complex heatmaps.
#BiocManager::install("ComplexHeatmap")
library(ComplexHeatmap)
# https://www.rdocumentation.org/packages/pheatmap/versions/1.0.12/topics/pheatmap
library(pheatmap)2.1 Functions
Some original and adapted functions can be found in the file that is silently processed here.
%% Additional functions
out <- ""
out <- paste(out,knit_child("005-Functions.Rmd", quiet=TRUE))2.2 File names
Usually we use a file management system under the pISA-tree framework. For simplicity, all files ( scripts, data ,… ) are in one directory.
Control of file source
usetest <- !TRUESample description file (aka phenodata)
pfn <- "./input/phenodata_subset_2023-03-08.txt"
files <- c(
"./input/data_hormonomics.txt"
, "./input/data_metabolomics.txt"
, "./input/data_qPCR.txt"
# , "./input/data_Phenomics.txt"
# , "./input/data_Proteomics.txt"
)Phenodata file name:
pfn## [1] "./input/phenodata_subset_2023-03-08.txt"Data file names
files ## [1] "./input/data_hormonomics.txt" "./input/data_metabolomics.txt"
## [3] "./input/data_qPCR.txt"For future use and labeling, we need text names of dataset objects.
datanames <- c(
"hormonomics"
, "metabolomics"
, "qPCR"
# , "phenomics"
# , "proteomics"
)
datanames## [1] "hormonomics" "metabolomics" "qPCR"Define groups to consider. In a small example, we will pick two groups, based on treatment:
useTreatment <- c("C","H")It is advisable to first read the phenodata, followed by actual data input. This enables smart selection of samples, based on the sample selection column with the assay name.
2.3 Phenodata
pfn## [1] "./input/phenodata_subset_2023-03-08.txt"#
phdata <- read.table(pfn
, header = TRUE
, sep = "\t"
, stringsAsFactors = FALSE
, row.names=1
)
dim(phdata)## [1] 56 30names(phdata)## [1] "Treatment"
## [2] "Harvest"
## [3] "SamplingDay"
## [4] "DaysOfStressH"
## [5] "DaysOfStressD"
## [6] "DaysOfStressW"
## [7] "DaysRecovery"
## [8] "Replicate"
## [9] "Sample.type"
## [10] "Date"
## [11] "Heat.Drought.Water.Recovery.Days"
## [12] "TreatmentxDatexPlant"
## [13] "TreatmentxSamplingDay"
## [14] "TreatmentxSamplingDayxReplicateNo"
## [15] "Comment"
## [16] "Num_Tubers"
## [17] "Total_Tubers_Weight"
## [18] "FW_SH_Total"
## [19] "DW_SH_Total"
## [20] "Fv.Fm"
## [21] "qL"
## [22] "deltaT"
## [23] "TOP.AREA"
## [24] "COMPACTNESS"
## [25] "WATER.CONSUMPTION"
## [26] "Proteomics"
## [27] "Transcriptomics"
## [28] "Metabolomics"
## [29] "Hormonomics"
## [30] "X_A_300_OverView.R"pdata <- phdataFilter out groups
pdata$Treatment## [1] "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C"
## [14] "C" "C" "C" "D" "D" "D" "D" "D" "D" "D" "D" "H" "H"
## [27] "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H"
## [40] "H" "HD" "HD" "HD" "HD" "HD" "HD" "HD" "HD" "W" "W" "W" "W"
## [53] "W" "W" "W" "W"pdata <- pdata[pdata$Treatment %in% useTreatment,]
pdata$Treatment## [1] "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C" "C"
## [17] "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H" "H"dim(pdata)## [1] 32 30Overview of selected samples:
addmargins(table(pdata$Treatment, pdata$SamplingDay))##
## 1 7 8 14 Sum
## C 4 4 4 4 16
## H 4 4 4 4 16
## Sum 8 8 8 8 32.treat <- unique(pdata$Treatment)
.days <- unique(pdata$SamplingDay)
.entry <- 0.5summary(pdata)## Treatment Harvest SamplingDay DaysOfStressH
## Length:32 Min. :1.00 Min. : 1.0 Min. : 0.00
## Class :character 1st Qu.:1.75 1st Qu.: 5.5 1st Qu.: 0.00
## Mode :character Median :2.50 Median : 7.5 Median : 0.50
## Mean :2.50 Mean : 7.5 Mean : 3.75
## 3rd Qu.:3.25 3rd Qu.: 9.5 3rd Qu.: 7.25
## Max. :4.00 Max. :14.0 Max. :14.00
## DaysOfStressD DaysOfStressW DaysRecovery Replicate
## Min. :0 Min. :0 Min. :0 Min. :1.00
## 1st Qu.:0 1st Qu.:0 1st Qu.:0 1st Qu.:1.75
## Median :0 Median :0 Median :0 Median :2.50
## Mean :0 Mean :0 Mean :0 Mean :2.50
## 3rd Qu.:0 3rd Qu.:0 3rd Qu.:0 3rd Qu.:3.25
## Max. :0 Max. :0 Max. :0 Max. :4.00
## Sample.type Date
## Length:32 Length:32
## Class :character Class :character
## Mode :character Mode :character
##
##
##
## Heat.Drought.Water.Recovery.Days TreatmentxDatexPlant
## Length:32 Length:32
## Class :character Class :character
## Mode :character Mode :character
##
##
##
## TreatmentxSamplingDay TreatmentxSamplingDayxReplicateNo
## Length:32 Length:32
## Class :character Class :character
## Mode :character Mode :character
##
##
##
## Comment Num_Tubers Total_Tubers_Weight FW_SH_Total
## Length:32 Mode:logical Mode:logical Min. :1
## Class :character NA's:32 NA's:32 1st Qu.:1
## Mode :character Median :1
## Mean :1
## 3rd Qu.:1
## Max. :1
## DW_SH_Total Fv.Fm qL deltaT TOP.AREA
## Min. :1 Min. :1 Min. :1 Min. :1 Min. :1
## 1st Qu.:1 1st Qu.:1 1st Qu.:1 1st Qu.:1 1st Qu.:1
## Median :1 Median :1 Median :1 Median :1 Median :1
## Mean :1 Mean :1 Mean :1 Mean :1 Mean :1
## 3rd Qu.:1 3rd Qu.:1 3rd Qu.:1 3rd Qu.:1 3rd Qu.:1
## Max. :1 Max. :1 Max. :1 Max. :1 Max. :1
## COMPACTNESS WATER.CONSUMPTION Proteomics Transcriptomics
## Min. :1 Min. :1 Min. :1 Min. :1
## 1st Qu.:1 1st Qu.:1 1st Qu.:1 1st Qu.:1
## Median :1 Median :1 Median :1 Median :1
## Mean :1 Mean :1 Mean :1 Mean :1
## 3rd Qu.:1 3rd Qu.:1 3rd Qu.:1 3rd Qu.:1
## Max. :1 Max. :1 Max. :1 Max. :1
## Metabolomics Hormonomics X_A_300_OverView.R
## Min. :1 Min. :1 Min. : 1.0
## 1st Qu.:1 1st Qu.:1 1st Qu.: 5.5
## Median :1 Median :1 Median : 7.5
## Mean :1 Mean :1 Mean : 7.5
## 3rd Qu.:1 3rd Qu.:1 3rd Qu.: 9.5
## Max. :1 Max. :1 Max. :14.0apply(pdata,2,function(x) summary(as.factor(x)))## $Treatment
## C H
## 16 16
##
## $Harvest
## 1 2 3 4
## 8 8 8 8
##
## $SamplingDay
## 1 7 8 14
## 8 8 8 8
##
## $DaysOfStressH
## 0 1 7 8 14
## 16 4 4 4 4
##
## $DaysOfStressD
## 0
## 32
##
## $DaysOfStressW
## 0
## 32
##
## $DaysRecovery
## 0
## 32
##
## $Replicate
## 1 2 3 4
## 8 8 8 8
##
## $Sample.type
## S
## 32
##
## $Date
## 2020-11-04 2020-11-10 2020-11-11 2020-11-17
## 8 8 8 8
##
## $Heat.Drought.Water.Recovery.Days
## 0_0_0_0 1_0_0_0 14_0_0_0 7_0_0_0 8_0_0_0
## 16 4 4 4 4
##
## $TreatmentxDatexPlant
## C_2020-11-04_1 C_2020-11-04_2 C_2020-11-04_3 C_2020-11-04_4
## 1 1 1 1
## C_2020-11-10_1 C_2020-11-10_2 C_2020-11-10_3 C_2020-11-10_4
## 1 1 1 1
## C_2020-11-11_1 C_2020-11-11_2 C_2020-11-11_3 C_2020-11-11_4
## 1 1 1 1
## C_2020-11-17_1 C_2020-11-17_2 C_2020-11-17_3 C_2020-11-17_4
## 1 1 1 1
## H_2020-11-04_1 H_2020-11-04_2 H_2020-11-04_3 H_2020-11-04_4
## 1 1 1 1
## H_2020-11-10_1 H_2020-11-10_2 H_2020-11-10_3 H_2020-11-10_4
## 1 1 1 1
## H_2020-11-11_1 H_2020-11-11_2 H_2020-11-11_3 H_2020-11-11_4
## 1 1 1 1
## H_2020-11-17_1 H_2020-11-17_2 H_2020-11-17_3 H_2020-11-17_4
## 1 1 1 1
##
## $TreatmentxSamplingDay
## C_1 C_14 C_7 C_8 H_1 H_14 H_7 H_8
## 4 4 4 4 4 4 4 4
##
## $TreatmentxSamplingDayxReplicateNo
## C_1_1 C_1_2 C_1_3 C_1_4 C_14_1 C_14_2 C_14_3 C_14_4 C_7_1 C_7_2
## 1 1 1 1 1 1 1 1 1 1
## C_7_3 C_7_4 C_8_1 C_8_2 C_8_3 C_8_4 H_1_1 H_1_2 H_1_3 H_1_4
## 1 1 1 1 1 1 1 1 1 1
## H_14_1 H_14_2 H_14_3 H_14_4 H_7_1 H_7_2 H_7_3 H_7_4 H_8_1 H_8_2
## 1 1 1 1 1 1 1 1 1 1
## H_8_3 H_8_4
## 1 1
##
## $Comment
## only for cor
## 32
##
## $Num_Tubers
## NA's
## 32
##
## $Total_Tubers_Weight
## NA's
## 32
##
## $FW_SH_Total
## 1
## 32
##
## $DW_SH_Total
## 1
## 32
##
## $Fv.Fm
## 1
## 32
##
## $qL
## 1
## 32
##
## $deltaT
## 1
## 32
##
## $TOP.AREA
## 1
## 32
##
## $COMPACTNESS
## 1
## 32
##
## $WATER.CONSUMPTION
## 1
## 32
##
## $Proteomics
## 1
## 32
##
## $Transcriptomics
## 1
## 32
##
## $Metabolomics
## 1
## 32
##
## $Hormonomics
## 1
## 32
##
## $X_A_300_OverView.R
## 1 7 8 14
## 8 8 8 82.4 Process data files
For this project we aim to integrate several multi-omics datasets. We have data on hormonomics, metabolomics, and qPCR:
%% {r} %% hormonomics <- read.table(file1, header=TRUE, sep="\t") %% metabolomics <- read.table(file2, header=TRUE, sep="\t") %% qPCR <- read.table(file3, header=TRUE, sep="\t") %%
Read all datafiles and assign them to named objects
for (i in 1:length(files)){
print(datanames[i])
assign(datanames[i], read.table(files[i], header=TRUE, sep="\t"))
print(head(get(datanames[i])))
}## [1] "hormonomics"
## SampleID IAA oxIAA IAA.Asp ABA PA DPA
## 1 C_S1_1 37.19565 61.49305 2.224072 36.78497 91.99991 45.63410
## 2 C_S1_2 45.86649 67.84222 1.990994 33.11733 92.61196 62.10651
## 3 C_S1_3 47.60516 52.49759 1.496438 41.66091 93.83119 55.06159
## 4 C_S1_4 37.55562 48.69611 2.240201 39.11995 91.35024 59.82576
## 5 C_S7_1 49.46230 76.79460 1.927162 80.00281 231.68757 178.08837
## 6 C_S7_2 78.91379 93.14059 1.856353 49.76028 166.08573 149.86757
## SA JA JA.Ile X9.10.dhJA X12.OH.JA cisOPDA
## 1 505.2129 2.687303 0.5525212 5.449105 16.13451 353.8608
## 2 519.3793 2.802456 0.5661384 3.700174 23.95458 402.7049
## 3 275.2972 4.761132 0.4273195 2.879761 27.93628 644.9688
## 4 628.0462 4.622662 0.2028412 5.165337 25.72584 750.3532
## 5 1314.9488 6.101443 0.6226329 5.010268 244.12270 1294.9082
## 6 731.2122 3.092070 0.3449961 8.373161 203.74167 873.4217
## [1] "metabolomics"
## SampleID Glukose Fructose Sucrose Starch Asp Glu Asn Ser
## 1 C_S1_1 2.13 2.70 3.449 22.06 1039.5 2514.0 177.8 597.9
## 2 C_S1_2 2.20 2.90 3.382 12.74 844.3 1966.4 167.8 498.1
## 3 C_S1_3 0.82 1.59 2.452 9.98 887.2 2067.8 167.0 441.1
## 4 C_S1_4 2.55 3.01 4.057 15.13 987.6 2347.9 172.3 537.6
## 5 C_S7_1 4.77 3.97 3.533 16.25 793.2 2109.0 276.9 368.5
## 6 C_S7_2 6.30 7.16 6.280 9.57 1391.6 3344.4 498.8 704.2
## Gln Gly His Arg Thr Ala Pro Tyr Val Met Ile Lys
## 1 497.8 137.8 20.7 26.9 225.4 702.5 48.6 25.3 54.1 7.3 48.8 26.0
## 2 408.8 104.6 13.3 29.1 208.5 495.5 57.3 22.1 51.3 6.9 47.0 21.8
## 3 400.1 92.1 17.1 29.5 216.1 514.6 53.5 24.4 52.9 8.6 54.3 26.5
## 4 465.7 117.2 16.8 24.9 252.0 653.1 58.6 22.3 58.4 7.9 52.9 26.7
## 5 265.7 68.7 13.7 38.3 188.6 296.4 85.8 31.2 73.1 4.7 60.4 28.4
## 6 680.9 101.2 19.4 63.9 302.4 664.6 135.7 40.6 96.3 8.6 80.6 33.1
## Leu Phe
## 1 18.8 119.0
## 2 15.7 88.0
## 3 19.5 86.8
## 4 20.1 111.0
## 5 27.4 98.3
## 6 27.1 171.2
## [1] "qPCR"
## SampleID RbohA SnRK2 ACO2 HSP70 PR1b RD29B
## 1 C_S1_1 1.346213 1.497998 0.150379 1.013451 0.324007 0.016995
## 2 C_S1_2 1.496014 1.627412 0.196017 1.067230 0.154344 0.046504
## 3 C_S1_3 1.262812 1.630533 0.440406 0.883357 0.269488 0.016995
## 4 C_S1_4 1.428252 1.530426 0.176572 1.042068 0.255647 0.082387
## 5 C_S7_1 1.404150 1.122600 0.537281 1.028170 0.226714 1.751881
## 6 C_S7_2 0.848707 0.725752 0.150857 0.640827 0.192341 0.113202
## X13.LOX P5CS ERF1 CAT1 CO SWEET SP6A
## 1 0.699873 3.647878 0.560424 0.639920 2.421594 0.816298 0.122374
## 2 0.660413 3.264675 0.637808 0.635107 5.563090 1.873813 0.238811
## 3 0.765764 2.151917 0.585558 0.687279 2.740914 0.930861 0.330151
## 4 0.734167 3.155558 0.663618 0.704880 2.469193 0.933900 0.122374
## 5 1.136201 0.862709 1.634810 0.811006 1.709219 1.494808 3.386457
## 6 0.540666 0.908966 1.239857 0.373886 1.580358 0.853875 0.810631
## M0ZJG3
## 1 1.211115
## 2 1.376397
## 3 1.007479
## 4 0.903495
## 5 2.357865
## 6 1.387190Check if all 3 objects are created
datanames## [1] "hormonomics" "metabolomics" "qPCR"datanames %in% ls()## [1] TRUE TRUE TRUE2.5 Combine datasets
Datasets for DIABLO need to be collected in a list, with rows corresponding to the same samples. The order of samples from shrinked phenodata will be enforced.
The first component of the list will be a grouping variable, indicating the conditions. We will create reasonable names for groups.
sday <- paste0(0,pdata$SamplingDay)
len <- nchar(sday)
sday <- substr(sday,len-1,len)
trt <- pdata$Treatment
what <- paste(trt,sday,sep="")
what## [1] "C01" "C01" "C01" "C01" "C07" "C07" "C07" "C07" "C08" "C08" "C08"
## [12] "C08" "C14" "C14" "C14" "C14" "H01" "H01" "H01" "H01" "H07" "H07"
## [23] "H07" "H07" "H08" "H08" "H08" "H08" "H14" "H14" "H14" "H14"X <- list(status= what)
names(X[[1]]) <- rownames(pdata)
X## $status
## C_S1_1 C_S1_2 C_S1_3 C_S1_4 C_S7_1 C_S7_2 C_S7_3 C_S7_4
## "C01" "C01" "C01" "C01" "C07" "C07" "C07" "C07"
## C_S8_1 C_S8_2 C_S8_3 C_S8_4 C_S14_1 C_S14_2 C_S14_3 C_S14_4
## "C08" "C08" "C08" "C08" "C14" "C14" "C14" "C14"
## H_S1_1 H_S1_2 H_S1_3 H_S1_4 H_S7_1 H_S7_2 H_S7_3 H_S7_4
## "H01" "H01" "H01" "H01" "H07" "H07" "H07" "H07"
## H_S8_1 H_S8_2 H_S8_3 H_S8_4 H_S14_1 H_S14_2 H_S14_3 H_S14_4
## "H08" "H08" "H08" "H08" "H14" "H14" "H14" "H14"print(addmargins(table(pdata$SamplingDay, what)), zero.print=".")## what
## C01 C07 C08 C14 H01 H07 H08 H14 Sum
## 1 4 . . . 4 . . . 8
## 7 . 4 . . . 4 . . 8
## 8 . . 4 . . . 4 . 8
## 14 . . . 4 . . . 4 8
## Sum 4 4 4 4 4 4 4 4 32print(addmargins(table(pdata$Treatment, what)), zero.print=".")## what
## C01 C07 C08 C14 H01 H07 H08 H14 Sum
## C 4 4 4 4 . . . . 16
## H . . . . 4 4 4 4 16
## Sum 4 4 4 4 4 4 4 4 32Put datasets into the list X and ensure that they all have same order of samples as in phenodata.
datanames## [1] "hormonomics" "metabolomics" "qPCR"i <- 1
for(i in 1:length(datanames)){
x <- get(datanames[i])
rownames(x) <- x[,1]
x <- x[,-1]
X[[i+1]] <- x[rownames(pdata),]
names(X)[i+1] <- datanames[i]
}
str(X)## List of 4
## $ status : Named chr [1:32] "C01" "C01" "C01" "C01" ...
## ..- attr(*, "names")= chr [1:32] "C_S1_1" "C_S1_2" "C_S1_3" "C_S1_4" ...
## $ hormonomics :'data.frame': 32 obs. of 12 variables:
## ..$ IAA : num [1:32] 37.2 45.9 47.6 37.6 49.5 ...
## ..$ oxIAA : num [1:32] 61.5 67.8 52.5 48.7 76.8 ...
## ..$ IAA.Asp : num [1:32] 2.22 1.99 1.5 2.24 1.93 ...
## ..$ ABA : num [1:32] 36.8 33.1 41.7 39.1 80 ...
## ..$ PA : num [1:32] 92 92.6 93.8 91.4 231.7 ...
## ..$ DPA : num [1:32] 45.6 62.1 55.1 59.8 178.1 ...
## ..$ SA : num [1:32] 505 519 275 628 1315 ...
## ..$ JA : num [1:32] 2.69 2.8 4.76 4.62 6.1 ...
## ..$ JA.Ile : num [1:32] 0.553 0.566 0.427 0.203 0.623 ...
## ..$ X9.10.dhJA: num [1:32] 5.45 3.7 2.88 5.17 5.01 ...
## ..$ X12.OH.JA : num [1:32] 16.1 24 27.9 25.7 244.1 ...
## ..$ cisOPDA : num [1:32] 354 403 645 750 1295 ...
## $ metabolomics:'data.frame': 32 obs. of 22 variables:
## ..$ Glukose : num [1:32] 2.13 2.2 0.82 2.55 4.77 6.3 7.24 3.09 6.34 9.49 ...
## ..$ Fructose: num [1:32] 2.7 2.9 1.59 3.01 3.97 7.16 5.41 4.04 8.52 7.75 ...
## ..$ Sucrose : num [1:32] 3.45 3.38 2.45 4.06 3.53 ...
## ..$ Starch : num [1:32] 22.06 12.74 9.98 15.13 16.25 ...
## ..$ Asp : num [1:32] 1040 844 887 988 793 ...
## ..$ Glu : num [1:32] 2514 1966 2068 2348 2109 ...
## ..$ Asn : num [1:32] 178 168 167 172 277 ...
## ..$ Ser : num [1:32] 598 498 441 538 368 ...
## ..$ Gln : num [1:32] 498 409 400 466 266 ...
## ..$ Gly : num [1:32] 137.8 104.6 92.1 117.2 68.7 ...
## ..$ His : num [1:32] 20.7 13.3 17.1 16.8 13.7 19.4 20.5 17.8 8.8 18.4 ...
## ..$ Arg : num [1:32] 26.9 29.1 29.5 24.9 38.3 63.9 38.6 47.3 54.7 67.2 ...
## ..$ Thr : num [1:32] 225 208 216 252 189 ...
## ..$ Ala : num [1:32] 702 496 515 653 296 ...
## ..$ Pro : num [1:32] 48.6 57.3 53.5 58.6 85.8 ...
## ..$ Tyr : num [1:32] 25.3 22.1 24.4 22.3 31.2 40.6 50.9 37.1 20.2 34.6 ...
## ..$ Val : num [1:32] 54.1 51.3 52.9 58.4 73.1 ...
## ..$ Met : num [1:32] 7.3 6.9 8.6 7.9 4.7 8.6 4.5 6.6 3.8 2.2 ...
## ..$ Ile : num [1:32] 48.8 47 54.3 52.9 60.4 80.6 62.7 63 29.9 48.3 ...
## ..$ Lys : num [1:32] 26 21.8 26.5 26.7 28.4 33.1 29.2 38.4 20.6 41.8 ...
## ..$ Leu : num [1:32] 18.8 15.7 19.5 20.1 27.4 27.1 21.3 26.3 38.5 45.7 ...
## ..$ Phe : num [1:32] 119 88 86.8 111 98.3 ...
## $ qPCR :'data.frame': 32 obs. of 14 variables:
## ..$ RbohA : num [1:32] 1.35 1.5 1.26 1.43 1.4 ...
## ..$ SnRK2 : num [1:32] 1.5 1.63 1.63 1.53 1.12 ...
## ..$ ACO2 : num [1:32] 0.15 0.196 0.44 0.177 0.537 ...
## ..$ HSP70 : num [1:32] 1.013 1.067 0.883 1.042 1.028 ...
## ..$ PR1b : num [1:32] 0.324 0.154 0.269 0.256 0.227 ...
## ..$ RD29B : num [1:32] 0.017 0.0465 0.017 0.0824 1.7519 ...
## ..$ X13.LOX: num [1:32] 0.7 0.66 0.766 0.734 1.136 ...
## ..$ P5CS : num [1:32] 3.648 3.265 2.152 3.156 0.863 ...
## ..$ ERF1 : num [1:32] 0.56 0.638 0.586 0.664 1.635 ...
## ..$ CAT1 : num [1:32] 0.64 0.635 0.687 0.705 0.811 ...
## ..$ CO : num [1:32] 2.42 5.56 2.74 2.47 1.71 ...
## ..$ SWEET : num [1:32] 0.816 1.874 0.931 0.934 1.495 ...
## ..$ SP6A : num [1:32] 0.122 0.239 0.33 0.122 3.386 ...
## ..$ M0ZJG3 : num [1:32] 1.211 1.376 1.007 0.903 2.358 ...names(X)## [1] "status" "hormonomics" "metabolomics" "qPCR"Check if sample names in all datasets match.
OK <- TRUE
for(i in 2:length(X)) {
print(ok <- all(names(X[[1]])==rownames(X[[i]])))
OK <- OK&ok
}## [1] TRUE
## [1] TRUE
## [1] TRUESample names in datasets match.
Put data into safe object DATA.
DATA <- XWe will also need the names of treatment groups.
groups <- unique(pdata$Treatment)
groups## [1] "C" "H"3 Multiomics data integration with DIABLO
CCDATA <- DATA
names(CCDATA)## [1] "status" "hormonomics" "metabolomics" "qPCR"write("Entering 035-DIABLO !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!", "bla.log", append=!TRUE)
write("commandArgs:", "bla.log", append=TRUE)
write(commandArgs(trailingOnly = TRUE), "bla.log",append=TRUE)
write("End commandArgs", "bla.log", append=TRUE)out <- ""
out <- paste(out,knit_child("035-DIABLO-2.Rmd", quiet=TRUE))
cat(out)Child: 035-DIABLO-2.Rmd ## DIABLO hormonomics, metabolomics, qPCR ## DIABLO
DIABLO from mixOmics enables integration of more than two datasets.
3.1 Organize data
Thre datasets are organized as a list of matrices with same samples as rows and variables in columns.
data <- CCDATA[-1]
str(data)## List of 3
## $ hormonomics :'data.frame': 32 obs. of 12 variables:
## ..$ IAA : num [1:32] 37.2 45.9 47.6 37.6 49.5 ...
## ..$ oxIAA : num [1:32] 61.5 67.8 52.5 48.7 76.8 ...
## ..$ IAA.Asp : num [1:32] 2.22 1.99 1.5 2.24 1.93 ...
## ..$ ABA : num [1:32] 36.8 33.1 41.7 39.1 80 ...
## ..$ PA : num [1:32] 92 92.6 93.8 91.4 231.7 ...
## ..$ DPA : num [1:32] 45.6 62.1 55.1 59.8 178.1 ...
## ..$ SA : num [1:32] 505 519 275 628 1315 ...
## ..$ JA : num [1:32] 2.69 2.8 4.76 4.62 6.1 ...
## ..$ JA.Ile : num [1:32] 0.553 0.566 0.427 0.203 0.623 ...
## ..$ X9.10.dhJA: num [1:32] 5.45 3.7 2.88 5.17 5.01 ...
## ..$ X12.OH.JA : num [1:32] 16.1 24 27.9 25.7 244.1 ...
## ..$ cisOPDA : num [1:32] 354 403 645 750 1295 ...
## $ metabolomics:'data.frame': 32 obs. of 22 variables:
## ..$ Glukose : num [1:32] 2.13 2.2 0.82 2.55 4.77 6.3 7.24 3.09 6.34 9.49 ...
## ..$ Fructose: num [1:32] 2.7 2.9 1.59 3.01 3.97 7.16 5.41 4.04 8.52 7.75 ...
## ..$ Sucrose : num [1:32] 3.45 3.38 2.45 4.06 3.53 ...
## ..$ Starch : num [1:32] 22.06 12.74 9.98 15.13 16.25 ...
## ..$ Asp : num [1:32] 1040 844 887 988 793 ...
## ..$ Glu : num [1:32] 2514 1966 2068 2348 2109 ...
## ..$ Asn : num [1:32] 178 168 167 172 277 ...
## ..$ Ser : num [1:32] 598 498 441 538 368 ...
## ..$ Gln : num [1:32] 498 409 400 466 266 ...
## ..$ Gly : num [1:32] 137.8 104.6 92.1 117.2 68.7 ...
## ..$ His : num [1:32] 20.7 13.3 17.1 16.8 13.7 19.4 20.5 17.8 8.8 18.4 ...
## ..$ Arg : num [1:32] 26.9 29.1 29.5 24.9 38.3 63.9 38.6 47.3 54.7 67.2 ...
## ..$ Thr : num [1:32] 225 208 216 252 189 ...
## ..$ Ala : num [1:32] 702 496 515 653 296 ...
## ..$ Pro : num [1:32] 48.6 57.3 53.5 58.6 85.8 ...
## ..$ Tyr : num [1:32] 25.3 22.1 24.4 22.3 31.2 40.6 50.9 37.1 20.2 34.6 ...
## ..$ Val : num [1:32] 54.1 51.3 52.9 58.4 73.1 ...
## ..$ Met : num [1:32] 7.3 6.9 8.6 7.9 4.7 8.6 4.5 6.6 3.8 2.2 ...
## ..$ Ile : num [1:32] 48.8 47 54.3 52.9 60.4 80.6 62.7 63 29.9 48.3 ...
## ..$ Lys : num [1:32] 26 21.8 26.5 26.7 28.4 33.1 29.2 38.4 20.6 41.8 ...
## ..$ Leu : num [1:32] 18.8 15.7 19.5 20.1 27.4 27.1 21.3 26.3 38.5 45.7 ...
## ..$ Phe : num [1:32] 119 88 86.8 111 98.3 ...
## $ qPCR :'data.frame': 32 obs. of 14 variables:
## ..$ RbohA : num [1:32] 1.35 1.5 1.26 1.43 1.4 ...
## ..$ SnRK2 : num [1:32] 1.5 1.63 1.63 1.53 1.12 ...
## ..$ ACO2 : num [1:32] 0.15 0.196 0.44 0.177 0.537 ...
## ..$ HSP70 : num [1:32] 1.013 1.067 0.883 1.042 1.028 ...
## ..$ PR1b : num [1:32] 0.324 0.154 0.269 0.256 0.227 ...
## ..$ RD29B : num [1:32] 0.017 0.0465 0.017 0.0824 1.7519 ...
## ..$ X13.LOX: num [1:32] 0.7 0.66 0.766 0.734 1.136 ...
## ..$ P5CS : num [1:32] 3.648 3.265 2.152 3.156 0.863 ...
## ..$ ERF1 : num [1:32] 0.56 0.638 0.586 0.664 1.635 ...
## ..$ CAT1 : num [1:32] 0.64 0.635 0.687 0.705 0.811 ...
## ..$ CO : num [1:32] 2.42 5.56 2.74 2.47 1.71 ...
## ..$ SWEET : num [1:32] 0.816 1.874 0.931 0.934 1.495 ...
## ..$ SP6A : num [1:32] 0.122 0.239 0.33 0.122 3.386 ...
## ..$ M0ZJG3 : num [1:32] 1.211 1.376 1.007 0.903 2.358 ...length(data)## [1] 3cimfn <- "cim.png"In addition, outcome, phenotypic state or in our case treatment can also be determined. We have combination of two treatments and four time points.
state <- factor(CCDATA[[1]])
table(state)## state
## C01 C07 C08 C14 H01 H07 H08 H14
## 4 4 4 4 4 4 4 4str(state)## Factor w/ 8 levels "C01","C07","C08",..: 1 1 1 1 2 2 2 2 3 3 ...
## - attr(*, "names")= chr [1:32] "C_S1_1" "C_S1_2" "C_S1_3" "C_S1_4" ...3.2 Initial analysis
Note: Additional insights can be found at http://mixomics.org/mixdiablo/diablo-tcga-case-study/.
3.2.1 Pairwise PLS comparisons
list.keepX = c(25, 25) # select arbitrary values of features to keep
list.keepY = c(25, 25)par(mfrow=c(2,2))
pairs <- combn(1:length(names(data)),2)
nms <- names(data)
outn <- ""
j <- 1
ncomp <- length(data)
cols <- c('orange1', 'lightgreen', "red")
if(length(data)==3) pick <- 1:3 else pick <- c(4,1:3)
cols <- c('orange1', 'brown1', 'lightgreen',"lightblue")[pick]
pchs <- c(16, 17, 15, 18)[pick]
j <- 1
cutoff <- 0.5
for(j in 1:ncol(pairs) ){
pair <- pairs[,j]
pair
X <- CCDATA[[pair[1]+1]]
Y <- CCDATA[[pair[2]+1]]
list.keepX <- rep(min(ncol(X), 25), ncomp)
list.keepY <- rep(min(ncol(Y), 25), ncomp)
x <- spls(X, Y, ncomp=ncomp, keepX = list.keepX, keepY = list.keepY)
assign(paste0("spls",j),x)
cat("\n",paste(nms[pair]), "\n")
cat("Results in:",paste0("spls",j),"\n")
cat("Correlation between pls variates:\n")
print(round(cor(x$variates$X, x$variates$Y),5))
#
plotVar(x, cutoff = cutoff, title = paste(nms[pair],collapse=", "),
legend = c(nms[pair][1], nms[pair][2]),
var.names = FALSE, style = 'graphics',
pch = pchs[pair], cex = c(2,2),
col = cols[pair])
}##
## hormonomics metabolomics
## Results in: spls1
## Correlation between pls variates:
## comp1 comp2 comp3
## comp1 0.91126 0.00000 0.00000
## comp2 0.13029 0.80764 0.00000
## comp3 0.00165 -0.00098 0.61826##
## hormonomics qPCR
## Results in: spls2
## Correlation between pls variates:
## comp1 comp2 comp3
## comp1 0.69330 0.00000 0.000
## comp2 -0.40812 0.63635 0.000
## comp3 -0.31053 0.39759 0.549##
## metabolomics qPCR
## Results in: spls3
## Correlation between pls variates:
## comp1 comp2 comp3
## comp1 0.74472 0.00000 0.00000
## comp2 0.38516 0.60146 0.00000
## comp3 0.27693 0.40129 0.61882
Circle Correlation Plots for pairwise PLS models on ADAPT data. At most top 25 features for each dimension with correlation above 0.5, are displayed.
3.2.2 Initial DIABLO model
Following the suggestion in the source, we will use design matrices with small values. This is supposed to keep low classification error rate.
entry <- .entry
design = matrix(entry, ncol = length(data), nrow = length(data),
dimnames = list(names(data), names(data)))
diag(design) = 0 # set diagonal to 0s
design## hormonomics metabolomics qPCR
## hormonomics 0.0 0.5 0.5
## metabolomics 0.5 0.0 0.5
## qPCR 0.5 0.5 0.0With a design in place, the initial DIABLO model can be generated. An arbitrarily high number of components (ncomp = 5) will be used.
# form basic DIABLO model
Y <- state
basic.diablo.model = block.splsda(X = data, Y = Y, ncomp = 5, design = design)## Design matrix has changed to include Y; each block will be
## linked to Y.######################################## test eval
knitr::opts_chunk$set(eval=!FALSE)3.2.3 Tuning the number of components
Details of tuning process can be found in the http://mixomics.org/mixdiablo/diablo-tcga-case-study/.
The process can be computer time consuming and was performed separately.
%% To choose the number of components for the final DIABLO model, the function perf() is run with 3-fold cross-validation repeated 10 times. Fold number should be smaller than minimal number of samples in groups. %% %% %% {r eval=FALSE} %% # Tuning of features can take a substantial amount of time. %% # Chunk not evaluated for this document. %% # %% # run component number tuning with repeated CV %% system.time(perf.diablo = perf(basic.diablo.model, validation = 'Mfold', %% folds = 3, nrepeat = 10)) %% %% plot(perf.diablo) # plot output of tuning %% %% %% %% %% {r eval=FALSE} %% # Tuning of features can take a substantial amount of time. %% # Chunk not evaluated for this document. %% # %% # set the optimal ncomp value %% ncomp <- perf.diablo$choice.ncomp$WeightedVote["Overall.BER", "centroids.dist"] %% # show the optimal choice for ncomp for each dist metric %% perf.diablo$choice.ncomp$WeightedVote %% %% %% For classification, the analysis suggests %% the number of components.
From previous tuning sessions one can conclude, that the classification rate stays roughly unchanged after two to four components, so we will set the number of components to the number of data sets:
ncomp <- length(data)
ncomp## [1] 33.2.4 Tuning the number of features
We choose the optimal number of variables to select in each data set using the tune.block.splsda() function, for a grid of keepX values for each type of omics. Note that the function has been set to favour a relatively small signature while allowing us to obtain a sufficient number of variables for downstream validation and/or interpretation. See ?tune.block.splsda.
%% The function tune is run with 10-fold cross validation, but repeated only once. Note that for a more thorough tuning process, provided sufficient computational time, we could increase the nrepeat argument. Here we have saved the results into an RData object that is available for download as the tuning can take a very long time, especially on lower end machines. %% %% %% {r } %% x <- list() %% for (i in 1:length(data)){ %% x[[i]] <- c( seq(5,min(30, ncol(data[[i]])) ,5)) %% } %% names(x) <- names(data) %% test.keepX <- x %% test.keepX %% #list (c(5:9, seq(10, 18, 2), seq(20,30,5)), %% # c(5:9, seq(10, 18, 2), seq(20,30,5)), %% # c(5:9, seq(10, 18, 2), seq(20,30,5))) %% %% %% %% %% {r eval=FALSE} %% # Tuning of features can take a substantial amount of time. %% # Chunk not evaluated for this document. %% # %% # run the feature selection tuning %% system.time(tune.model <- tune.block.splsda(X = data, Y = Y, ncomp = ncomp, cpus=4, %% test.keepX = test.keepX, design = design, %% validation = 'Mfold', folds = 3, nrepeat = 1, %% dist = "centroids.dist") %% ) %% %% %% {r eval=FALSE} %% # Tuning of features can take a substantial amount of time. %% # Chunk not evaluated for this document. %% # %% # run the feature selection tuning %% system.time(tune.model <- tune.block.splsda(X = data, Y = Y, ncomp = ncomp, cpus=4, %% test.keepX = test.keepX, design = design, %% validation = 'loo', folds = 3, nrepeat = 1, %% dist = "centroids.dist") %% ) %% %% %% The number of features to select on each component is returned in %% {r eval=FALSE} %% # Tuning of features can take a substantial amount of time. %% # Chunk not evaluated for this document. %% # %% list.keepX = tune.model$choice.keepX # set the optimal values of features to retain %% list.keepX %%
Previous analyses suggest the following list:
$metabolomics
[1] 10 10 5
$hormonomics
[1] 5 5 10
$qPCR
[1] 10 10 5
We have decided to keep 10 variates for each component.
keepX <- list(
metabolomics = rep(10, ncomp),
hormonomics = rep(10, ncomp),
qPCR = rep(10, ncomp)
)
list.keepX = list()
for (i in 1:length(data)) list.keepX[[i]] <- keepX[[names(data)[i]]]
names(list.keepX) <- names(data)
list.keepX## $hormonomics
## [1] 10 10 10
##
## $metabolomics
## [1] 10 10 10
##
## $qPCR
## [1] 10 10 103.3 Final model
The final DIABLO model is run as:
# set the optimised DIABLO model
final.diablo.model = block.splsda(X = data, Y = as.factor(state)
, ncomp = ncomp
, keepX = list.keepX
, design = design)## Design matrix has changed to include Y; each block will be
## linked to Y.The selected variables can be extracted with the function selectVar(), for example in each block, as seen below. Note that the stability of selected variables can be extracted from the output of the perf() function.
# the features selected from components
for (comp in 1:ncomp){
cat("\nComponent ", comp,":\n")
for(i in 1:length(data)){
cat(names(data)[i],"\n")
print(selectVar(final.diablo.model, comp = comp)[[i]]$name)
}
}##
## Component 1 :
## hormonomics
## [1] "DPA" "SA" "PA" "X12.OH.JA" "X9.10.dhJA"
## [6] "JA.Ile" "ABA" "IAA" "IAA.Asp" "cisOPDA"
## metabolomics
## [1] "Glukose" "Fructose" "Val" "Ile" "Tyr" "Lys"
## [7] "His" "Gln" "Pro" "Met"
## qPCR
## [1] "X13.LOX" "PR1b" "CAT1" "SP6A" "M0ZJG3" "HSP70"
## [7] "SWEET" "RbohA" "SnRK2" "ERF1"
##
## Component 2 :
## hormonomics
## [1] "ABA" "oxIAA" "IAA" "cisOPDA" "JA.Ile"
## [6] "PA" "IAA.Asp" "SA" "DPA" "X12.OH.JA"
## metabolomics
## [1] "Starch" "Ser" "Asn" "His" "Met" "Arg"
## [7] "Sucrose" "Gly" "Pro" "Glukose"
## qPCR
## [1] "SP6A" "SnRK2" "RD29B" "CO" "P5CS" "PR1b" "HSP70"
## [8] "M0ZJG3" "ACO2" "RbohA"
##
## Component 3 :
## hormonomics
## [1] "JA.Ile" "JA" "oxIAA" "IAA.Asp" "X9.10.dhJA"
## [6] "DPA" "PA" "SA" "IAA" "cisOPDA"
## metabolomics
## [1] "Met" "Gln" "Ala" "Leu" "Phe" "Gly" "Glu" "Ile" "Arg" "Asp"
## qPCR
## [1] "ACO2" "PR1b" "X13.LOX" "RD29B" "CO" "M0ZJG3"
## [7] "SnRK2" "P5CS" "ERF1" "SWEET"3.4 Sample plots
plotDIABLO() is a diagnostic plot to check whether the correlation between components from each data set has been maximised as specified in the design matrix. We specify which dimension to be assessed with the ncomp argument.
for(comp in 1:ncomp){
plotDiablo(final.diablo.model, ncomp = comp)
title(paste("Component",comp), adj=0.1, line=-1, outer=TRUE)
}
The sample plot with the plotIndiv() function projects each sample into the space spanned by the components of each block. Clustering of the samples can be assessed with this plot.
plind <- plotIndiv(final.diablo.model,
ind.names = FALSE,
legend = TRUE,
title = 'DIABLO Sample Plots',
guide="none",
ellipse = TRUE
)## Warning: It is deprecated to specify `guide = FALSE` to remove a
## guide. Please use `guide = "none"` instead.
In the arrow plot below, the start of the arrow indicates the centroid between all data sets for a given sample and the tips of the arrows indicate the location of that sample in each block. Such graphics highlight the agreement between all data sets at the sample level. While somewhat difficult to interpret, even qualitatively, this arrow plot shows proximities of C01 and H01 (both day 1), C07 and C08, and H07 and H08 ( both a day apart). While C samples are in forth quadrant ( D1 < 0, D2 > 0), H samples have ( D1 < 0, D2 < 0) except H14 that is separated on the positive part of Dimension 1.
plotArrow(final.diablo.model, ind.names = FALSE, legend = TRUE,
title = paste(groups,collapse=", ")
)
3.5 Variable plots
Several graphical outputs are available to visualise and mine the associations between the selected variables.
The best starting point to evaluate the correlation structure between variables is with the correlation circle plot. A majority of the qPCR variables are positively correlated only with the first component. The hormonomics and metabolomics variables seem to separate along first two dimensions. These first two components correlate highly with the selected variables from the all three dataset. From this, the correlation of each selected feature from all three datasets can be evaluated based on their proximity.
#if(length(data)==3) pick <- 1:3 else pick <- c(4,1:3)
#cols <- c('orange1', 'brown1', 'lightgreen',"lightblue")[pick]
#pchs <- c(16, 17, 15, 18)[pick]
cols <- c('orange1', 'brown1', 'lightgreen')
pchs <- c(16, 17, 15)
plotVar(final.diablo.model, var.names = FALSE,
style = 'graphics', legend = TRUE
, pch = pchs, cex = rep(2,length(data))
, col = cols
)
The circos plot is exclusive to integrative frameworks and represents the correlations between variables of different types, represented on the side quadrants. It seems that the qPCR variables are almost entirely negatively correlated with the other two dataframes. Just few from metabolomics and hormonomics are positively correlated. Note that these correlations are above a value of 0.7 (cutoff = 0.7). All interpretations made above are only relevant for features with very strong correlations.
Plot variables
#plotVar(res, cutoff=0.5, legend = TRUE, overlap=!FALSE, style='graphics')
#plotVar(res, cutoff=0.5, legend = TRUE, overlap=FALSE, style='graphics')
plotVar(final.diablo.model, cutoff=0.5, legend = TRUE, comp=c(1,2), overlap=FALSE, style='ggplot2', col=cols)
plotVar(final.diablo.model, cutoff=0.5, legend = TRUE, comp=c(2,3), overlap=FALSE, col=cols)
circosPlot(final.diablo.model, cutoff = 0.7, line = TRUE,
color.blocks= cols,
color.cor = c(3,2), size.labels = 1
, xpd=TRUE)
3.6 Relevance networks
Another visualisation of the correlations between the different types of variables is the relevance network, which is also built on the similarity matrix (as is the circos plot). Colour represent variable type.
blocks <- combn(length(data),2)
j <- 1
cutoff <- 0.8
out35a <- ""
for(j in 1:ncol(blocks)){
out35a <- paste( out35a, knit_child("035a-DIABLO-network.Rmd", quiet=!TRUE))
if(interactive()) readline()
}
cat(out35a)3.6.1 hormonomics and metabolomics
nfn <- paste0("network-035a-",paste(names(data)[blocks[,j]], collapse="-"),"-",cutoff*10)
#nfn <- paste0("network-035a-",j,"-",cutoff*10)
nfn## [1] "network-035a-hormonomics-metabolomics-8"write(nfn, "bla.log", append=TRUE)png(paste0(nfn,".png"), res = 600, width = 4000, height = 4000)
nw <- network(final.diablo.model
, blocks = blocks[,j]
, color.node = cols[blocks[,j]]
, cutoff = cutoff
, shape.node = "rectangle"
, save = "png"
, name.save = nfn
)
#title(main=paste(names(data)[blocks[,j]], sep=", "),
#sub=paste("Cutoff = ",cutoff))
#
#dev.off()Cutoff = 0.8
network-035a-hormonomics-metabolomics-8
3.6.2 hormonomics and qPCR
nfn <- paste0("network-035a-",paste(names(data)[blocks[,j]], collapse="-"),"-",cutoff*10)
#nfn <- paste0("network-035a-",j,"-",cutoff*10)
nfn## [1] "network-035a-hormonomics-qPCR-8"write(nfn, "bla.log", append=TRUE)png(paste0(nfn,".png"), res = 600, width = 4000, height = 4000)
nw <- network(final.diablo.model
, blocks = blocks[,j]
, color.node = cols[blocks[,j]]
, cutoff = cutoff
, shape.node = "rectangle"
, save = "png"
, name.save = nfn
)
#title(main=paste(names(data)[blocks[,j]], sep=", "),
#sub=paste("Cutoff = ",cutoff))
#
#dev.off()Cutoff = 0.8
network-035a-hormonomics-qPCR-8
3.6.3 metabolomics and qPCR
nfn <- paste0("network-035a-",paste(names(data)[blocks[,j]], collapse="-"),"-",cutoff*10)
#nfn <- paste0("network-035a-",j,"-",cutoff*10)
nfn## [1] "network-035a-metabolomics-qPCR-8"write(nfn, "bla.log", append=TRUE)png(paste0(nfn,".png"), res = 600, width = 4000, height = 4000)
nw <- network(final.diablo.model
, blocks = blocks[,j]
, color.node = cols[blocks[,j]]
, cutoff = cutoff
, shape.node = "rectangle"
, save = "png"
, name.save = nfn
)
#title(main=paste(names(data)[blocks[,j]], sep=", "),
#sub=paste("Cutoff = ",cutoff))
#
#dev.off()Cutoff = 0.8
network-035a-metabolomics-qPCR-8
3.7 Multipartite network
cutoff <- 0.0
x <- final.diablo.model
layout.fun <- NULL
label <- paste(.treat, collapse=", ")
out35b <- ""
out35b <- paste( out35b, knit_child("035b-multipartite-network.Rmd", quiet=TRUE))
cat(out35b)3.7.1 Cutoff = 0
ndata <- length(data)
lbl <- gsub(", ","-",label)
nfn <- paste("network-035b",lbl,cutoff*10,sep="-")
#png(nfn, res = 600, width = 4000, height = 4000)
write(nfn, "bla.log", append=TRUE)set.seed(1234)
nw <- my.network(x
, blocks = 1:ndata
, color.node = cols
, cutoff = cutoff
, shape.node = "rectangle"
, layout = layout.fun
, save = "png"
, name.save = nfn
)
# title( #main=paste(names(data), sep=", "),
# sub=paste("Cutoff = ",cutoff))
# title(label,adj=0.8,outer=TRUE,line=-1)
# legend("bottomright", pch=15,pt.cex=2,col=cols, legend=names(data),
# bty="n")
# text(ly[,1],ly[,2],names(V(nw$gR)))
#dev.off()
network-035b-C-H-0
# Save network layout in ly, used by my.layout function.
if(exists(deparse(substitute(nw)))) ly <- nw$layout else ly <- NULLcutoff <- 0.8
x <- final.diablo.model
label <- paste(.treat, collapse=", ")
out35b <- ""
out35b <- paste( out35b, knit_child("035b-multipartite-network.Rmd", quiet=TRUE))
cat(out35b)3.7.2 Cutoff = 0.8
ndata <- length(data)
lbl <- gsub(", ","-",label)
nfn <- paste("network-035b",lbl,cutoff*10,sep="-")
#png(nfn, res = 600, width = 4000, height = 4000)
write(nfn, "bla.log", append=TRUE)set.seed(1234)
nw <- my.network(x
, blocks = 1:ndata
, color.node = cols
, cutoff = cutoff
, shape.node = "rectangle"
, layout = layout.fun
, save = "png"
, name.save = nfn
)
# title( #main=paste(names(data), sep=", "),
# sub=paste("Cutoff = ",cutoff))
# title(label,adj=0.8,outer=TRUE,line=-1)
# legend("bottomright", pch=15,pt.cex=2,col=cols, legend=names(data),
# bty="n")
# text(ly[,1],ly[,2],names(V(nw$gR)))
#dev.off()
network-035b-C-H-8
3.8 Visualize loadings
The function “plotLoadings” visualises the loading weights of each selected variable on each component and each data set. The colour indicates the class in which the variable has the maximum level of expression “contrib = ‘max’” using the median “method = ‘median’”. Figure below depicts the loading values for each dimension.
for(i in 1:ncomp)
plotLoadings(final.diablo.model, comp = i, contrib = 'max', method = 'median')
3.9 Clustered image map ( Heatmap )
The cimDIABLO() function is a clustered image map specifically implemented to represent the multi-omics molecular signature expression for each sample. From figure below the areas of homogeneous expression levels for a set of samples across a set of features can be determined. For instance, the H14 samples were the only group to show extremely high levels of expression for a specific set of genes and metabolites. This indicates these features are fairly discriminating for this subtype.
cimfn <- "cim.png"png(cimfn, res = 600, width = 4000, height = 4000)
cimDiablo(final.diablo.model, size.legend=0.7)
dev.off()## pdf
## 2
cim.png
3.10 AUC and ROC plots
An AUC plot per block can also be obtained using the function auroc(). The interpretation of this output may not be particularly insightful in relation to the performance evaluation of our methods, but can complement the statistical analysis.
par(mfrow=c(2,2))
for(i in 1:length(data))
auc.splsda = auroc(final.diablo.model, roc.block = names(data[i]),
roc.comp = 1, print = FALSE)
Save finil DIABLO model for future use in networks.
res <- final.diablo.modelEstimate classification error rate. The error rate should drop by more components used.
# run component number tuning with repeated CV
system.time(perf.diablo <- perf(res, validation = 'Mfold',
folds = 3, nrepeat = 10))## user system elapsed
## 9.34 0.26 10.21plot(perf.diablo) # plot output of tuning
3.11 Names of kept variables
# the features selected to form components
for (comp in 1:ncomp){
cat("\nComponent ", comp,":\n")
for(i in 1:length(data)){
cat(names(data)[i],"\n")
print(selectVar(res, comp = comp)[[i]]$name)
}
}##
## Component 1 :
## hormonomics
## [1] "DPA" "SA" "PA" "X12.OH.JA" "X9.10.dhJA"
## [6] "JA.Ile" "ABA" "IAA" "IAA.Asp" "cisOPDA"
## metabolomics
## [1] "Glukose" "Fructose" "Val" "Ile" "Tyr" "Lys"
## [7] "His" "Gln" "Pro" "Met"
## qPCR
## [1] "X13.LOX" "PR1b" "CAT1" "SP6A" "M0ZJG3" "HSP70"
## [7] "SWEET" "RbohA" "SnRK2" "ERF1"
##
## Component 2 :
## hormonomics
## [1] "ABA" "oxIAA" "IAA" "cisOPDA" "JA.Ile"
## [6] "PA" "IAA.Asp" "SA" "DPA" "X12.OH.JA"
## metabolomics
## [1] "Starch" "Ser" "Asn" "His" "Met" "Arg"
## [7] "Sucrose" "Gly" "Pro" "Glukose"
## qPCR
## [1] "SP6A" "SnRK2" "RD29B" "CO" "P5CS" "PR1b" "HSP70"
## [8] "M0ZJG3" "ACO2" "RbohA"
##
## Component 3 :
## hormonomics
## [1] "JA.Ile" "JA" "oxIAA" "IAA.Asp" "X9.10.dhJA"
## [6] "DPA" "PA" "SA" "IAA" "cisOPDA"
## metabolomics
## [1] "Met" "Gln" "Ala" "Leu" "Phe" "Gly" "Glu" "Ile" "Arg" "Asp"
## qPCR
## [1] "ACO2" "PR1b" "X13.LOX" "RD29B" "CO" "M0ZJG3"
## [7] "SnRK2" "P5CS" "ERF1" "SWEET"One would like to reduce the number of nodes, especially for proteomics data. One option is to reduce datasets in a way to keep only the variables in the selectVars in original data in . We will keep variables from the first two components.
keptVars <- unique(c(
selectVar(res, comp=1)[[1]]$name
,selectVar(res, comp=2)[[1]]$name
)
)
which(keptVars%in%selectVar(res, comp=1)[[1]]$name)## [1] 1 2 3 4 5 6 7 8 9 10which(keptVars%in%selectVar(res, comp=2)[[1]]$name)## [1] 1 2 3 4 6 7 8 9 10 113.12 Visualise variables
Loadings
sapply(res$loadings, head, 30)## $hormonomics
## comp1 comp2 comp3
## IAA 0.036703482 -0.40678302 0.02662456
## oxIAA 0.000000000 0.41472146 -0.46097105
## IAA.Asp -0.007071215 -0.19836112 -0.38748591
## ABA 0.216332456 0.49851046 0.00000000
## PA 0.426177444 0.25246990 0.07019303
## DPA 0.549700457 -0.08274318 0.14734983
## SA 0.428211919 -0.17502093 0.03899104
## JA 0.000000000 0.00000000 0.48879193
## JA.Ile 0.246436078 -0.32453847 -0.55019009
## X9.10.dhJA 0.297909166 0.00000000 -0.25753363
## X12.OH.JA 0.367626768 0.05459029 0.00000000
## cisOPDA 0.003133045 0.40638498 -0.02327900
##
## $metabolomics
## comp1 comp2 comp3
## Glukose 0.48451843 0.0007744579 0.00000000
## Fructose 0.44913578 0.0000000000 0.00000000
## Sucrose 0.00000000 0.1755425740 0.00000000
## Starch 0.00000000 0.6230690186 0.00000000
## Asp 0.00000000 0.0000000000 0.02433324
## Glu 0.00000000 0.0000000000 -0.08664505
## Asn 0.00000000 -0.3852103155 0.00000000
## Ser 0.00000000 0.4187171275 0.00000000
## Gln -0.13859433 0.0000000000 0.52431197
## Gly 0.00000000 0.0875580979 0.12358545
## His 0.21679051 -0.3308628088 0.00000000
## Arg 0.00000000 -0.2436655212 -0.02652000
## Thr 0.00000000 0.0000000000 0.00000000
## Ala 0.00000000 0.0000000000 0.41741363
## Pro 0.11913529 0.0723114386 0.00000000
## Tyr 0.34922488 0.0000000000 0.00000000
## Val 0.37933829 0.0000000000 0.00000000
## Met -0.07239333 -0.2748085404 0.62202620
## Ile 0.35208370 0.0000000000 0.08509517
## Lys 0.29674894 0.0000000000 0.00000000
## Leu 0.00000000 0.0000000000 -0.27616600
## Phe 0.00000000 0.0000000000 0.23740522
##
## $qPCR
## comp1 comp2 comp3
## RbohA 0.16466558 -0.01682425 0.000000000
## SnRK2 0.13112994 -0.30963253 -0.139934444
## ACO2 0.00000000 -0.04461440 -0.883294093
## HSP70 0.24795487 -0.11801339 0.000000000
## PR1b 0.37477829 0.12308322 -0.306943422
## RD29B 0.00000000 0.28522220 0.155469415
## X13.LOX 0.58349667 0.00000000 0.168233520
## P5CS 0.00000000 -0.14974981 0.066857223
## ERF1 0.09174938 0.00000000 -0.065022964
## CAT1 0.37449858 0.00000000 0.000000000
## CO 0.00000000 -0.15196379 0.150498594
## SWEET 0.21148675 0.00000000 0.004392953
## SP6A 0.34570655 0.85834408 0.000000000
## M0ZJG3 0.31681955 -0.09567284 0.148846821
##
## $Y
## comp1 comp2 comp3
## C01 -0.346770705 0.03865545 0.25532621
## C07 -0.110583348 0.11426169 0.19174216
## C08 -0.008904022 0.38818375 0.02515787
## C14 0.063004541 0.64332045 -0.38125662
## H01 -0.287945254 -0.14936480 0.29508918
## H07 -0.116690109 -0.40997461 0.17110929
## H08 -0.065417492 -0.44511069 -0.76872677
## H14 0.873306389 -0.17997122 0.21155868#plotLoadings(res, comp = 1, method = 'median')
#plotLoadings(res, comp = 1, method = 'median', contrib="max")
for( i in 1:ncomp)
plotLoadings(res, comp = i, method = 'median', contrib="max")
3.13 Plot variables
#plotVar(res, cutoff=0.5, legend = TRUE, overlap=!FALSE, style='graphics')
#plotVar(res, cutoff=0.5, legend = TRUE, overlap=FALSE, style='graphics')
plotVar(res, cutoff=0.5, legend = TRUE, comp=c(1,2), overlap=FALSE, style='ggplot2', col=cols)
plotVar(res, cutoff=0.5, legend = TRUE, comp=c(2,3), overlap=FALSE, col=cols)
4 Differential networks
Here we will show differential networks between treatments.
cutoffs <- c(0.7)
pairs <- combn(1:length(names(res$X)),2)
outn <- ""
j <- 4
cutoff <- 0.5
for(j in 1:ncol(pairs) ){
pair <- pairs[,j]
X <- data[[pair[1]]]
Y <- data[[pair[2]]]
datasets <- names(data)[pair]
outn <- paste( outn, knit_child("023-prepare-networkdiff.Rmd", quiet=TRUE))
for(cutoff in cutoffs){
outn <- paste( outn, knit_child("035-Network.Rmd", quiet=TRUE))
}
}
cat(outn)size.variables <- 1
sim <-circosPlot(final.diablo.model, cutoff = 0.5, line = TRUE,
color.blocks= cols,
color.cor = c(3,2), size.labels = 1
, size.variables = size.variables
, xpd=TRUE)
circosPlot(final.diablo.model, cutoff = 0.75, line = TRUE,
color.blocks= cols,
color.cor = c(3,2), size.labels = 1
, size.variables = size.variables
, xpd=TRUE)
circosPlot(final.diablo.model, cutoff = 0.9, line = TRUE,
color.blocks= cols,
color.cor = c(3,2), size.labels = 1
, size.variables = size.variables
, xpd=TRUE)
5 Networks
We will prepare partial models for each treatment and treatment combination.
5.1 Network for C.
filter <- pdata$Treatment %in% .treat[1]
XX1 <- lapply(CCDATA, function(x) if(is.null(dim(x))) x[filter] else x[filter,])
table(XX1$status)##
## C01 C07 C08 C14
## 4 4 4 4res1 <- block.splsda(X = XX1[-1]
, Y = as.factor(XX1[[1]])
, ncomp = ncomp
, keepX = list.keepX
, design = design
)## Design matrix has changed to include Y; each block will be
## linked to Y.cutoff <- 0.0
x <- res1
layout.fun <- NULL
label <-.treat[1]
out23b <- ""
out23b <- paste( out23b, knit_child("035b-multipartite-network.Rmd", quiet=TRUE))
N1 <- nw
cat(out23b)5.1.1 Cutoff = 0
ndata <- length(data)
lbl <- gsub(", ","-",label)
nfn <- paste("network-035b",lbl,cutoff*10,sep="-")
#png(nfn, res = 600, width = 4000, height = 4000)
write(nfn, "bla.log", append=TRUE)set.seed(1234)
nw <- my.network(x
, blocks = 1:ndata
, color.node = cols
, cutoff = cutoff
, shape.node = "rectangle"
, layout = layout.fun
, save = "png"
, name.save = nfn
)
# title( #main=paste(names(data), sep=", "),
# sub=paste("Cutoff = ",cutoff))
# title(label,adj=0.8,outer=TRUE,line=-1)
# legend("bottomright", pch=15,pt.cex=2,col=cols, legend=names(data),
# bty="n")
# text(ly[,1],ly[,2],names(V(nw$gR)))
#dev.off()
network-035b-C-0
Save network layout for further plots, used by layout function my.layout.
ly <- nw$layoutcutoff <- 0.7
x <- res1
layout.fun <- my.layout
label <- .treat[1]
out23b <- ""
out23b <- paste( out23b, knit_child("035b-multipartite-network.Rmd", quiet=TRUE))
cat(out23b)5.1.2 Cutoff = 0.7
ndata <- length(data)
lbl <- gsub(", ","-",label)
nfn <- paste("network-035b",lbl,cutoff*10,sep="-")
#png(nfn, res = 600, width = 4000, height = 4000)
write(nfn, "bla.log", append=TRUE)set.seed(1234)
nw <- my.network(x
, blocks = 1:ndata
, color.node = cols
, cutoff = cutoff
, shape.node = "rectangle"
, layout = layout.fun
, save = "png"
, name.save = nfn
)
# title( #main=paste(names(data), sep=", "),
# sub=paste("Cutoff = ",cutoff))
# title(label,adj=0.8,outer=TRUE,line=-1)
# legend("bottomright", pch=15,pt.cex=2,col=cols, legend=names(data),
# bty="n")
# text(ly[,1],ly[,2],names(V(nw$gR)))
#dev.off()
network-035b-C-7
5.2 Network for H.
filter <- pdata$Treatment %in% .treat[2]
XX2 <- lapply(CCDATA, function(x) if(is.null(dim(x))) x[filter] else x[filter,])
table(XX2$status)##
## H01 H07 H08 H14
## 4 4 4 4res2 <- block.splsda(X = XX2[-1]
, Y = as.factor(XX2[[1]])
, ncomp = ncomp
, keepX = list.keepX
, design = design
)## Design matrix has changed to include Y; each block will be
## linked to Y.cutoff <- 0.0
x <- res2
layout.fun <- NULL
label <- .treat[2]
out23b <- ""
out23b <- paste( out23b, knit_child("035b-multipartite-network.Rmd", quiet=TRUE))
N2 <- nw
cat(out23b)5.2.1 Cutoff = 0
ndata <- length(data)
lbl <- gsub(", ","-",label)
nfn <- paste("network-035b",lbl,cutoff*10,sep="-")
#png(nfn, res = 600, width = 4000, height = 4000)
write(nfn, "bla.log", append=TRUE)set.seed(1234)
nw <- my.network(x
, blocks = 1:ndata
, color.node = cols
, cutoff = cutoff
, shape.node = "rectangle"
, layout = layout.fun
, save = "png"
, name.save = nfn
)
# title( #main=paste(names(data), sep=", "),
# sub=paste("Cutoff = ",cutoff))
# title(label,adj=0.8,outer=TRUE,line=-1)
# legend("bottomright", pch=15,pt.cex=2,col=cols, legend=names(data),
# bty="n")
# text(ly[,1],ly[,2],names(V(nw$gR)))
#dev.off()
network-035b-H-0
Save layout for further plots, used by layout function my.layout.
ly <- nw$layoutcutoff <- 0.7
x <- res2
layout.fun <- my.layout
label <- .treat[2]
out23b <- ""
out23b <- paste( out23b, knit_child("035b-multipartite-network.Rmd", quiet=TRUE))
cat(out23b)5.2.2 Cutoff = 0.7
ndata <- length(data)
lbl <- gsub(", ","-",label)
nfn <- paste("network-035b",lbl,cutoff*10,sep="-")
#png(nfn, res = 600, width = 4000, height = 4000)
write(nfn, "bla.log", append=TRUE)set.seed(1234)
nw <- my.network(x
, blocks = 1:ndata
, color.node = cols
, cutoff = cutoff
, shape.node = "rectangle"
, layout = layout.fun
, save = "png"
, name.save = nfn
)
# title( #main=paste(names(data), sep=", "),
# sub=paste("Cutoff = ",cutoff))
# title(label,adj=0.8,outer=TRUE,line=-1)
# legend("bottomright", pch=15,pt.cex=2,col=cols, legend=names(data),
# bty="n")
# text(ly[,1],ly[,2],names(V(nw$gR)))
#dev.off()
network-035b-H-7
Save network file for combined and single treatments. Networks are in objects res, res1 and res2.
write("Mid diablo 5 41 !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!", "bla.log", append=TRUE)5.3 Network for C and H.
# Complete network, cutoff = 0, both
datasets <- names(CCDATA[-1])
ndatasets<- length(datasets)
#
N12 <- network(res
, cutoff = 0
, blocks = 1:ndatasets
, shape.node = c("rectangle")
, save = "png"
, name.save="network-CH"
)
#
e <- extractEdges2(N12)
colnames(e)[ncol(e)] <- paste(.treat, collapse=".")
head(e)## edge group1 from
## ho.IAA_me.Glukose ho.IAA_me.Glukose hormonomics IAA
## ho.oxIAA_me.Glukose ho.oxIAA_me.Glukose hormonomics oxIAA
## ho.IAA.Asp_me.Glukose ho.IAA.Asp_me.Glukose hormonomics IAA.Asp
## ho.ABA_me.Glukose ho.ABA_me.Glukose hormonomics ABA
## ho.PA_me.Glukose ho.PA_me.Glukose hormonomics PA
## ho.DPA_me.Glukose ho.DPA_me.Glukose hormonomics DPA
## group2 to C.H
## ho.IAA_me.Glukose metabolomics Glukose -0.08555827
## ho.oxIAA_me.Glukose metabolomics Glukose 0.51707118
## ho.IAA.Asp_me.Glukose metabolomics Glukose -0.22176715
## ho.ABA_me.Glukose metabolomics Glukose 0.80887195
## ho.PA_me.Glukose metabolomics Glukose 0.86161713
## ho.DPA_me.Glukose metabolomics Glukose 0.73483118tail(e)## edge group1 from group2 to
## me.Val_qP.M0ZJG3 me.Val_qP.M0ZJG3 metabolomics Val qPCR M0ZJG3
## me.Met_qP.M0ZJG3 me.Met_qP.M0ZJG3 metabolomics Met qPCR M0ZJG3
## me.Ile_qP.M0ZJG3 me.Ile_qP.M0ZJG3 metabolomics Ile qPCR M0ZJG3
## me.Lys_qP.M0ZJG3 me.Lys_qP.M0ZJG3 metabolomics Lys qPCR M0ZJG3
## me.Leu_qP.M0ZJG3 me.Leu_qP.M0ZJG3 metabolomics Leu qPCR M0ZJG3
## me.Phe_qP.M0ZJG3 me.Phe_qP.M0ZJG3 metabolomics Phe qPCR M0ZJG3
## C.H
## me.Val_qP.M0ZJG3 0.9022587
## me.Met_qP.M0ZJG3 -0.3590730
## me.Ile_qP.M0ZJG3 0.8768180
## me.Lys_qP.M0ZJG3 0.8442707
## me.Leu_qP.M0ZJG3 0.5974332
## me.Phe_qP.M0ZJG3 0.4424355dim(e)## [1] 714 6# treatment 1
e1 <- extractEdges2(N1)
colnames(e1)[ncol(e1)] <- .treat[1]
head(e1)## edge group1 from
## ho.IAA_me.Glukose ho.IAA_me.Glukose hormonomics IAA
## ho.oxIAA_me.Glukose ho.oxIAA_me.Glukose hormonomics oxIAA
## ho.IAA.Asp_me.Glukose ho.IAA.Asp_me.Glukose hormonomics IAA.Asp
## ho.ABA_me.Glukose ho.ABA_me.Glukose hormonomics ABA
## ho.PA_me.Glukose ho.PA_me.Glukose hormonomics PA
## ho.DPA_me.Glukose ho.DPA_me.Glukose hormonomics DPA
## group2 to C
## ho.IAA_me.Glukose metabolomics Glukose -0.009706936
## ho.oxIAA_me.Glukose metabolomics Glukose 0.407917620
## ho.IAA.Asp_me.Glukose metabolomics Glukose -0.268229896
## ho.ABA_me.Glukose metabolomics Glukose 0.740096225
## ho.PA_me.Glukose metabolomics Glukose 0.896262542
## ho.DPA_me.Glukose metabolomics Glukose 0.829405769dim(e1)## [1] 662 6e <- merge(e,e1, sort=FALSE, all=TRUE)
head(e)## edge group1 from group2 to
## 1 ho.IAA_me.Glukose hormonomics IAA metabolomics Glukose
## 2 ho.oxIAA_me.Glukose hormonomics oxIAA metabolomics Glukose
## 3 ho.IAA.Asp_me.Glukose hormonomics IAA.Asp metabolomics Glukose
## 4 ho.ABA_me.Glukose hormonomics ABA metabolomics Glukose
## 5 ho.PA_me.Glukose hormonomics PA metabolomics Glukose
## 6 ho.DPA_me.Glukose hormonomics DPA metabolomics Glukose
## C.H C
## 1 -0.08555827 -0.009706936
## 2 0.51707118 0.407917620
## 3 -0.22176715 -0.268229896
## 4 0.80887195 0.740096225
## 5 0.86161713 0.896262542
## 6 0.73483118 0.829405769tail(e)## edge group1 from group2 to C.H
## 709 me.His_qP.HSP70 metabolomics His qPCR HSP70 0.8217718
## 710 me.Lys_qP.ACO2 metabolomics Lys qPCR ACO2 0.6368664
## 711 ho.oxIAA_me.Lys hormonomics oxIAA metabolomics Lys 0.2842323
## 712 me.Lys_qP.RbohA metabolomics Lys qPCR RbohA 0.5059654
## 713 me.Lys_qP.SnRK2 metabolomics Lys qPCR SnRK2 0.8284052
## 714 me.Lys_qP.P5CS metabolomics Lys qPCR P5CS 0.8220844
## C
## 709 NA
## 710 NA
## 711 NA
## 712 NA
## 713 NA
## 714 NA# treatment 2
.treat[2]## [1] "H"e2 <- extractEdges2(N2)
colnames(e2)[ncol(e2)] <- .treat[2]
head(e2)## edge group1 from
## ho.IAA_me.Glukose ho.IAA_me.Glukose hormonomics IAA
## ho.oxIAA_me.Glukose ho.oxIAA_me.Glukose hormonomics oxIAA
## ho.IAA.Asp_me.Glukose ho.IAA.Asp_me.Glukose hormonomics IAA.Asp
## ho.ABA_me.Glukose ho.ABA_me.Glukose hormonomics ABA
## ho.PA_me.Glukose ho.PA_me.Glukose hormonomics PA
## ho.DPA_me.Glukose ho.DPA_me.Glukose hormonomics DPA
## group2 to H
## ho.IAA_me.Glukose metabolomics Glukose -0.03135486
## ho.oxIAA_me.Glukose metabolomics Glukose 0.34316156
## ho.IAA.Asp_me.Glukose metabolomics Glukose -0.24733014
## ho.ABA_me.Glukose metabolomics Glukose 0.87529961
## ho.PA_me.Glukose metabolomics Glukose 0.88467893
## ho.DPA_me.Glukose metabolomics Glukose 0.89945125dim(e2)## [1] 688 6e <- merge(e,e2, sort=FALSE, all=TRUE)
head(e)## edge group1 from group2 to
## 1 ho.IAA_me.Glukose hormonomics IAA metabolomics Glukose
## 2 ho.oxIAA_me.Glukose hormonomics oxIAA metabolomics Glukose
## 3 ho.IAA.Asp_me.Glukose hormonomics IAA.Asp metabolomics Glukose
## 4 ho.ABA_me.Glukose hormonomics ABA metabolomics Glukose
## 5 ho.PA_me.Glukose hormonomics PA metabolomics Glukose
## 6 ho.DPA_me.Glukose hormonomics DPA metabolomics Glukose
## C.H C H
## 1 -0.08555827 -0.009706936 -0.03135486
## 2 0.51707118 0.407917620 0.34316156
## 3 -0.22176715 -0.268229896 -0.24733014
## 4 0.80887195 0.740096225 0.87529961
## 5 0.86161713 0.896262542 0.88467893
## 6 0.73483118 0.829405769 0.89945125tail(e)## edge group1 from group2 to C.H C H
## 735 me.Thr_qP.HSP70 metabolomics Thr qPCR HSP70 NA NA 0.2569343
## 736 me.Thr_qP.CAT1 metabolomics Thr qPCR CAT1 NA NA 0.3463942
## 737 me.Thr_qP.ERF1 metabolomics Thr qPCR ERF1 NA NA 0.1878546
## 738 me.Thr_qP.P5CS metabolomics Thr qPCR P5CS NA NA 0.2701877
## 739 me.Thr_qP.CO metabolomics Thr qPCR CO NA NA 0.3305915
## 740 me.Thr_qP.M0ZJG3 metabolomics Thr qPCR M0ZJG3 NA NA 0.3471071#write("Mid diablo 5 !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!", "bla.log", append=TRUE)Compose file name and necessary information for network export file
file <- paste0("network-",paste(.treat, collapse="_"),"-",paste(datasets, collapse="_"),".txt")
label0 <- paste(paste(.treat, collapse=", "),"|",paste(datasets, collapse=", "),"; cutoff =",0)
title <- label0
sets <- 1:length(DATA)
suffix <- paste0(substr(names(DATA),1,2)[sets[-1]],collapse="-")write("Mid diablo 6 !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!", "bla.log", append=TRUE)
write(file.path(suffix,file), "bla.log", append=TRUE)
write(file, "bla.log", append=TRUE)length(str(e))## 'data.frame': 740 obs. of 8 variables:
## $ edge : chr "ho.IAA_me.Glukose" "ho.oxIAA_me.Glukose" "ho.IAA.Asp_me.Glukose" "ho.ABA_me.Glukose" ...
## $ group1: chr "hormonomics" "hormonomics" "hormonomics" "hormonomics" ...
## $ from : chr "IAA" "oxIAA" "IAA.Asp" "ABA" ...
## $ group2: chr "metabolomics" "metabolomics" "metabolomics" "metabolomics" ...
## $ to : chr "Glukose" "Glukose" "Glukose" "Glukose" ...
## $ C.H : num -0.0856 0.5171 -0.2218 0.8089 0.8616 ...
## $ C : num -0.00971 0.40792 -0.26823 0.7401 0.89626 ...
## $ H : num -0.0314 0.3432 -0.2473 0.8753 0.8847 ...## [1] 05.4 Export edges table
#e <- data.frame(x=1:10,y=1:10)
#my.write.table(e, file="network.txt",meta=FALSE)
write.table(e, file = file, na="0")Table with edges for networks based on combined treatments (C, H) and single treatments (C) and (H) is exported as a text file. This table can be used for inspection and filtering out edges based on selected cutoff. Missing edges are labeled as weight 0. This enables numeric filtration in other visualization or analysis files (e.g. Excel).
write("End diablo 7 !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!", "bla.log", append=TRUE)write("From 035-DIABLO !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!", "bla.log", append=TRUE)6 SessionInfo
Windows 10 x64 (build 19045)
R version 4.0.2 (2020-06-22) Platform: x86_64-w64-mingw32/x64 (64-bit) Running under: Windows 10 x64 (build 19045)
Matrix products: default
locale: [1] LC_COLLATE=Slovenian_Slovenia.1250 [2] LC_CTYPE=Slovenian_Slovenia.1250
[3] LC_MONETARY=Slovenian_Slovenia.1250 [4] LC_NUMERIC=C
[5] LC_TIME=Slovenian_Slovenia.1250
system code page: 1252
attached base packages: [1] grid stats graphics utils datasets grDevices [7] methods base
other attached packages: [1] pheatmap_1.0.12 ComplexHeatmap_2.6.2 igraph_1.2.6
[4] mixOmics_6.14.0 ggplot2_3.3.5 lattice_0.22-5
[7] MASS_7.3-60.0.1 knitr_1.43 rmarkdown_2.21
loaded via a namespace (and not attached): [1] ggrepel_0.9.0 Rcpp_1.0.7 circlize_0.4.15
[4] tidyr_1.1.2 corpcor_1.6.9 png_0.1-7
[7] digest_0.6.35 RSpectra_0.16-0 R6_2.5.1
[10] plyr_1.8.6 stats4_4.0.2 ellipse_0.4.2
[13] evaluate_0.21 highr_0.8 pillar_1.4.7
[16] GlobalOptions_0.1.2 rlang_1.1.1 jquerylib_0.1.4
[19] S4Vectors_0.28.1 GetoptLong_1.0.5 Matrix_1.6-5
[22] labeling_0.4.2 rARPACK_0.11-0 stringr_1.4.0
[25] munsell_0.5.0 compiler_4.0.2 xfun_0.39
[28] pkgconfig_2.0.3 BiocGenerics_0.36.0 shape_1.4.6
[31] htmltools_0.5.2 tidyselect_1.1.0 tibble_3.0.4
[34] gridExtra_2.3 IRanges_2.24.1 matrixStats_1.2.0
[37] crayon_1.3.4 dplyr_1.0.2 withr_3.0.0
[40] jsonlite_1.8.8 gtable_0.3.0 lifecycle_0.2.0
[43] magrittr_2.0.1 scales_1.1.1 stringi_1.5.3
[46] farver_2.0.3 reshape2_1.4.4 bslib_0.3.1
[49] ellipsis_0.3.1 generics_0.1.0 vctrs_0.4.1
[52] rjson_0.2.20 RColorBrewer_1.1-2 tools_4.0.2
[55] Cairo_1.5-15 glue_1.4.2 purrr_0.3.4
[58] parallel_4.0.2 fastmap_1.1.1 yaml_2.2.1
[61] clue_0.3-60 colorspace_1.4-1 cluster_2.1.0
[64] sass_0.4.0